Linked Data
ClinVar Variation Id:
159839
ClinVar RCV Id:
RCV000147417
RCV000247824
RCV000285029
RCV000377071
RCV000380122
RCV001085166
RCV000323206
dbSNP Id:
rs138704724
ExAC:
19:38948856 C / T
gnomAD v2:
19-38948856-C-T
gnomAD v3:
19-38458216-C-T
gnomAD v4:
19-38458216-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38458216C>T , CM000681.2:g.38458216C>T | GRCh38 |
| NC_000019.9:g.38948856C>T , CM000681.1:g.38948856C>T | GRCh37 |
| NC_000019.8:g.43640696C>T | NCBI36 |
| NG_008866.1:g.29517C>T , LRG_766:g.29517C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.2091C>T | ENSP00000471601.2:p.Ala697= | |
| ENST00000359596.8:c.2091C>T MANE Select | ENSP00000352608.2:p.Ala697= | |
| ENST00000355481.8:c.2091C>T | ENSP00000347667.3:p.Ala697= | |
| ENST00000359596.7:c.2091C>T | ENSP00000352608.2:p.Ala697= | |
| ENST00000360985.7:c.2091C>T | ENSP00000354254.4:p.Ala697= | |
| NM_000540.2:c.2091C>T , LRG_766t1:c.2091C>T | NP_000531.2:p.Ala697= | |
| NM_001042723.1:c.2091C>T | NP_001036188.1:p.Ala697= | |
| XM_006723317.1:c.2091C>T | XP_006723380.1:p.Ala697= | |
| XM_006723319.1:c.2091C>T | XP_006723382.1:p.Ala697= | |
| XM_011527204.1:c.2088C>T | XP_011525506.1:p.Ala696= | |
| XM_011527205.1:c.2091C>T | XP_011525507.1:p.Ala697= | |
| XM_006723317.2:c.2091C>T | XP_006723380.1:p.Ala697= | |
| XM_006723319.2:c.2091C>T | XP_006723382.1:p.Ala697= | |
| XM_011527205.2:c.2091C>T | XP_011525507.1:p.Ala697= | |
| XR_001753735.1:n.2174C>T | ||
| NM_000540.3:c.2091C>T MANE Select | NP_000531.2:p.Ala697= | |
| NM_001042723.2:c.2091C>T | NP_001036188.1:p.Ala697= |